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V V Ionasescu

Showing results (1-10 of 30) with videos related to

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Muscle & Nerve|March 1, 1995
Charcot-Marie-Tooth neuropathies: from clinical description to molecular geneticsV V Ionasescu
Cell Biology International|June 30, 2000
X-linked Charcot-Marie-Tooth disease and connexin32V V Ionasescu
Biochemical and Biophysical Research Communications|April 14, 1980
Alterations in lipid turnover in developing muscleA Sandra, V V Ionasescu
Human Molecular Genetics|September 1, 1993
Mutation of the myelin P0 gene in Charcot-Marie-Tooth neuropathy type 1BK Hayasaka, G Takada, V V Ionasescu
Neurology|August 1, 1986
Prenatal diagnosis of Duchenne muscular dystrophy based on Xp21.2 deletionV V Ionasescu, C Searby, R Ionasescu
Muscle & Nerve|November 1, 1993
Screening of dominantly inherited Charcot-Marie-Tooth neuropathiesV V Ionasescu, R Ionasescu, C Searby
Acta Neurologica Scandinavica|June 1, 1989
Manifesting carrier of Becker muscular dystrophy (BMD): clinical and recombinant DNA studiesV V Ionasescu, C C Searby, R Ionasescu
Journal of Medical Genetics|December 1, 1996
Dejerine-Sottas disease with sensorineural hearing loss, nystagmus, and peripheral facial nerve weakness: de novo dominant point mutation of the PMP22 geneV V Ionasescu, C Searby, S A Greenberg
Developmental Medicine and Child Neurology|June 1, 1988
Serial position memory of boys with Duchenne muscular dystrophyS W Anderson, D K Routh, V V Ionasescu
Neurology|September 1, 1995
Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 geneV V Ionasescu, R Ionasescu, C Searby, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Muscle & Nerve|March 1, 1995
Charcot-Marie-Tooth neuropathies: from clinical description to molecular geneticsV V Ionasescu
Cell Biology International|June 30, 2000
X-linked Charcot-Marie-Tooth disease and connexin32V V Ionasescu
Biochemical and Biophysical Research Communications|April 14, 1980
Alterations in lipid turnover in developing muscleA Sandra, V V Ionasescu
Human Molecular Genetics|September 1, 1993
Mutation of the myelin P0 gene in Charcot-Marie-Tooth neuropathy type 1BK Hayasaka, G Takada, V V Ionasescu
Neurology|August 1, 1986
Prenatal diagnosis of Duchenne muscular dystrophy based on Xp21.2 deletionV V Ionasescu, C Searby, R Ionasescu
Muscle & Nerve|November 1, 1993
Screening of dominantly inherited Charcot-Marie-Tooth neuropathiesV V Ionasescu, R Ionasescu, C Searby
Acta Neurologica Scandinavica|June 1, 1989
Manifesting carrier of Becker muscular dystrophy (BMD): clinical and recombinant DNA studiesV V Ionasescu, C C Searby, R Ionasescu
Journal of Medical Genetics|December 1, 1996
Dejerine-Sottas disease with sensorineural hearing loss, nystagmus, and peripheral facial nerve weakness: de novo dominant point mutation of the PMP22 geneV V Ionasescu, C Searby, S A Greenberg
Developmental Medicine and Child Neurology|June 1, 1988
Serial position memory of boys with Duchenne muscular dystrophyS W Anderson, D K Routh, V V Ionasescu
Neurology|September 1, 1995
Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 geneV V Ionasescu, R Ionasescu, C Searby, et al.
Pageof 3